Drug recall
p-Chip Wand Reader
FDA recall event 92483 · Class II · p-Chip Corporation
Key facts
| Event ID | 92483 |
|---|---|
| Recall numbers | Z-1693-2023 |
| Recalling firm | p-Chip Corporation |
| Product type | Devices |
| Products | p-Chip Wand Reader |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA Requested |
| Reason for recall | The laser operation might fall under a higher laser class. |
| Initiation date | Mar 3, 2021 |
| Report date | Jun 21, 2023 |
| City | Chicago |
| State | IL |
| Country | United States |
| FEI number | 3027394592 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: